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Seroma clinical trials

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NCT ID: NCT04185480 Completed - Seroma Clinical Trials

Evaluating Hemopatch in Reducing Seroma Related Complications Following Axillary Lymph Node Dissection: a Pilot Study

HEIDI
Start date: June 16, 2020
Phase: N/A
Study type: Interventional

To evaluate if the use of Hemopatch in axillary lymph node dissection shows potential in reducing clinically significant seroma and seroma related complications, which might serve as a basis for a randomized controlled trial.

NCT ID: NCT04080934 Recruiting - Pain, Postoperative Clinical Trials

Breaststroke Swimming After Breast Cancer Treatment/Surgery as a Means of Treatment for Seroma, Lymphedema, and Chronic Arm and Chest Pain

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Following surgery and treatment for breast cancer, many patients experience swelling of lymph nodes (lymphedema) or accumulation of fluid (seroma) that can cause pain, restrict movement, and reduce quality of life. Current treatments include massage, pressure dressings, and drainage, but these are often ineffective and do not last. Physical activity, in particular swimming, has been linked to improvement in lymphedema/seroma symptoms, but more research is required to determine whether or not this type of treatment is effective.

NCT ID: NCT04035590 Recruiting - Breast Cancer Clinical Trials

Seroma Reduction and Drain Free Mastectomy

SARA
Start date: June 26, 2020
Phase: N/A
Study type: Interventional

To prove that omitting drains after mastectomy and flap fixation does not contribute to higher incidence of seroma formation and therefore reducing patient disutility such as seroma aspirations and visits to the outpatient clinic, as well as reducing seroma related wound complications.

NCT ID: NCT03773575 Recruiting - Amputation Clinical Trials

Evaluation of Closed Incision Negative Pressure Dressing (PREVENA) to Prevent Lower Extremity Amputation Wound Complications

PREVENA-AMP
Start date: January 15, 2019
Phase: N/A
Study type: Interventional

This study is a prospective, multi-center, two-arm, unblinded, and randomized controlled trial with a goal of evaluating the impact of a closed incision negative pressure dressing (PREVENA) on incidence of post-operative wound complications and medical costs in patients undergoing lower extremity amputation.

NCT ID: NCT03738527 Recruiting - Breast Cancer Clinical Trials

SEroma Reduction pOst MAstectomy "SEROMA Study"

SEROMA
Start date: October 7, 2019
Phase: Phase 4
Study type: Interventional

This is a pilot study to evaluate the feasibility of conducting a larger trial to determine if the use of intraoperative topical tranexamic acid (TXA) decreases the rate of post-operative hematomas and seromas in breast cancer patients after their mastectomy. In other words, the investigators want to determine if applying TXA inside the surgical wound before it is closed helps reduce blood or serous fluid accumulation at the operative site. Dependent on the results of this study, a further larger trial may or may not take place. Post-operative seromas and hematomas are common complications of mastectomy surgery not only leading to infection, discomfort, wound dehiscence or emergency room visits; they also delay in some instances post-operative adjuvant radiotherapy. Establishing whether or not topical TXA is an effective strategy to decrease those complications can potentially impact positively the breast cancer treatment. To achieve this aim, this randomized pilot study will first determine whether a larger multicenter study if feasible. This study will replicate a formal randomized trial at a smaller scale in a single center in order to assess the recruitment and randomization process, as well as provide preliminary results for our research question.

NCT ID: NCT03665883 Completed - Hernia, Inguinal Clinical Trials

Use of Diathermy Versus Blunt Dissection in TEP for Inguinal Hernia

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

There is a long debate whether monopoloar or blunt dissection should be adopted in TEP to minimise the chance of seroma formation. This study aims at study the effect on seroma formation (and pre-peritoneal drain output) by 2 techniques in randomised controlled trial.

NCT ID: NCT03650868 Completed - Breast Cancer Clinical Trials

The Effect of Thoracal Paravertebral Block on Seroma Reduction in Breast Surgery

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Thoracal paravertebral block (TPVB) is a commonly prefferred regional anesthesia technique to provide postoperative analgesia. In addition, the successful use of TPVB is reported for some seroma related pain cases. Postoperative analgesia in breast surgery is a difficult and overworked issue due to etensive surgery and complex innervation of the breast and in addition to this complex mechanisms, seroma accumulation has a negative effect for patients postoperatively. With this study, the investigators aimed to study the effect of TPVB on seroma reduction for breast cancer surgery.

NCT ID: NCT03647930 Completed - Seroma Clinical Trials

The Effect of Arista on Post-Operative Bleeding and Wound Drainage Following Mastectomy

Start date: May 15, 2012
Phase: N/A
Study type: Interventional

Study aim was to evaluate topical MPH on the risk of post-mastectomy seroma formation as measured by total drain output and total drain days.

NCT ID: NCT03598712 Recruiting - Breast Cancer Clinical Trials

Local Compression Seroma DIminution Objective (CLODIS)

CLODIS
Start date: November 18, 2018
Phase: Phase 3
Study type: Interventional

This study evaluates the impact of local compression by chest bandage on the number of seroma punctures in patients treated by mastectomy with or without lymphadectomy. Half of the participants will have local compression by chest bandage in addition to seroma punctures while the other half will only have punctures.

NCT ID: NCT03590704 Completed - Seroma Clinical Trials

Safety of the Use of Compressive Taping in Seroma

Start date: June 6, 2017
Phase: N/A
Study type: Interventional

Seroma is the most common complication at the beginning of healing after surgery for breast cancer treatment. Its incidence varies in the literature from 2.5 to 90% and is defined as a collection of serous fluid that develops through skin flaps in the dead space after mastectomy or axillary dissection. The physiopathology for seroma formation has not yet been fully understood, but appears to be multifactorial with surgery being the main factor. Although seroma formation is not a threat to life, it can lead to important morbidity due to associated with necrosis, dehiscence, predisposition to sepsis, reduction of shoulder functions due to muscle weakness due to restriction of movement, prolonging the recovery period and, consequently, leading to delay in adjuvant therapy. The best seroma treatment is still not well defined in the literature and the compressive therapy aims to rebalance fluid exchange between the lymphatic system and blood, having as effects the increase of the interstitial pressure, the improvement of the effectiveness of muscular work, increased resistance of the skin and prevention new collection of interstitial fluid. Recently, the Kinesio® Taping method were inserted into clinical practice for its ability to reduce pain and local swelling. Objective: To evaluate the safety of taping in the seroma after surgical treatment of breast cancer. Methodology: This is a pre and post-clinical application of taping on the seroma in women submitted to surgical treatment for breast cancer in the Cancer Hospital III / INCA. The intervention was performed by applying the compression bandage over the seroma region for an average of five days, when the reassessment was performed.